Evidence map›Paper›PMID 35412170›Full record

ArticleBiochemical genetics2022

CDC42 Regulates Cell Proliferation and Apoptosis in Bladder Cancer via the IQGAP3-Mediated Ras/ERK Pathway.

Gang Li, Yu Wang, Xiao-Bo Guo, Bo Zhao

Abstract read
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In one paragraph

Article in Biochemical genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Gang LiDepartment of Urology, Heji Hospital Affiliated to Changzhi Medical College, No. 271, Taihang East Street, Changzhi, 046011, Shanxi, People's Republic of China. ggaanngiaan456@163.com.ORCID http://orcid.org/0000-0002-2461-5400
Yu WangDepartment of Pathology, Heji Hospital Affiliated to Changzhi Medical College, Changzhi, 046011, Shanxi, People's Republic of China.
Xiao-Bo GuoDepartment of Urology, Heji Hospital Affiliated to Changzhi Medical College, No. 271, Taihang East Street, Changzhi, 046011, Shanxi, People's Republic of China.
Bo ZhaoDepartment of Urology, Heji Hospital Affiliated to Changzhi Medical College, No. 271, Taihang East Street, Changzhi, 046011, Shanxi, People's Republic of China.
Changzhi Medical College · CN

Funding

scientific and technological innovation programs of higher education institutions in shanxi 2019L0697
6 · The paper itself

Abstract

Bladder cancer (BC) is the most common malignant tumour of the urinary system. The current conventional treatments for BC have certain limitations. It is very urgent and necessary to find new treatment strategies for BC. Our study elucidated the underlying regulatory mechanisms of cell division control protein 42 homologue (CDC42) to regulate the development of BC. Quantitative real-time polymerase chain reaction, Western blot, immunofluorescence and immunohistochemistry were used to assess the expression of CDC42 and IQ motif-containing GTPase-activating protein 3 (IQGAP3) in BC tissues and BC cells. We induced the knockdown or overexpression by transfecting sh-CDC42 or oe-IQGAP3 into BC cells. In addition, cell proliferation and apoptosis were evaluated by cell counting kit-8 and flow cytometry assays, respectively. Moreover, proteins involved in the rat sarcoma (Ras)/extracellular regulated protein kinase (ERK) pathway were determined by Western blot. The expression of CDC42 and IQGAP3 was markedly upregulated in both BC tissues and BC cells. CDC42 silencing downregulated the expression of IQGAP3 and suppressed the Ras/ERK pathway. In addition, CDC42 silencing markedly promoted apoptosis and inhibited proliferation in BC cells. Further experiments showed that overexpression of IQGAP3 dramatically abolished the bioeffects mediated by CDC42 silencing on the proliferation and apoptosis of BC cells. All our results suggested that CDC42 promoted the Ras/ERK pathway by regulating IQGAP3, thus enhancing cell proliferation and suppressing cell apoptosis in BC cells and ultimately participating in the pathogenesis of BC.

Indexed as

cdc42 GTP-Binding ProteinGTPase-Activating ProteinsUrinary Bladder NeoplasmsApoptosisCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemProtein Kinasescdc42 GTP-Binding ProteinCDC42 protein, humanGTPase-Activating ProteinsIQGAP3 protein, humanProtein KinasesBladder cancerCDC42Cell apoptosisCell proliferationIQGAP3Ras/ERK pathway

Identifiers

PMID35412170
OpenAlexW4223490429

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.